Integrative Skin Science Research is seeking a motivated individual to conduct and support

clinical research focused on holistic and integrative therapies as well as pharmaceutical

interventions.

Our research program is expanding, and we are seeking candidates to join our reputable

research team.

This candidate will work closely with Principal Investigator (PI) and Sub-investigators as well as

Clinical Research Coordinators, and Research Fellows. Specific duties will include but not

limited to: recruiting and screening study subjects, overseeing study visit procedures in

accordance with FDA Regulations and Good Clinical Practices, and assisting with overseeing

CRFs.

ISSR operates Monday through Friday \| 8:00am - 5:00pm

In this role you will be expected to perform the following duties:

Preparing essential clinical trial documents
Tracking, distributing and filing documents when they are returned
Management of key study related meetings including; agenda preparation, arranging
Supporting clinical research staff within the department
Coordination of the translation of key patient facing documents
Managing trial supplies
Composition of Investigator Site File (ISF)
Creating and maintaining study contact lists for study team and sites
Setting up mail merges
Archiving documents
Sending study newsletters to sites
Assisting with the management of safety including SUSAR reporting
Organising accommodation and flights regarding IM meetings, site visits etc
Understanding of trackers and formulas
Quality checking CRO eTMF systems and flagging any findings to the relevant person

*Must be able to occasionally work hours other than Monday through Friday 8:00 a.m. to 5:00

p.m. due to operational needs. Must be willing to work a flexible schedule as necessary to meet

deadlines.

Job Type:

Full Time

Benefits:

Physical Setting:

Clinic Work Location: Sacramento

Job Type:

Full-time

Pay:

$20-25 8 hour shift

Work Location

: In person

Clinical Trials Administrator

Job Description